Sucralfate
- Product NDC
- 80425-0213
- 11-digit product format
- 804250213
- Labeler code
- 80425
- Product ID
- 80425-0213_2a9a6113-0a2f-6005-e063-6294a90abc5e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Advanced Rx Pharmacy of Tennessee, LLC
- Application
- NDA018333
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2023-01-03
- Substance
- SUCRALFATE
- Active strength
- 1 g/1
- Pharmacologic classes
- Aluminum Complex [EPC], Organometallic Compounds [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| XX73205DH5 | SUCRALFATE | 54182-58-0 | SUCRALFATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 80425-0213-1 | 80425021301 | 30 TABLET in 1 BOTTLE (80425-0213-1) | 30 tablet | 2023-01-03 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Sucralfate Tablets | Advanced Rx Pharmacy of Tennessee, LLC | 2024-12-31 | HUMAN PRESCRIPTION DRUG LABEL | 3 |